115984-46-8Relevant articles and documents
Palladium-catalyzed aldol-type condensation by enol esters with SnCl2
Masuyama, Yoshiro,Sakai, Tatsuya,Kurusu, Yasuhiko
, p. 653 - 656 (1992)
Using PdCl2(PhCN)2-SnCl2, enol esters caused aldol-type condensation with aldehydes at 50°C in acetonitrile to produce (E)-α,β-unsaturated carbonyl compounds. Cyclic enol ester such as α-angelicalactone also reacted with aldehydes under the same conditions to afford γ-substituted β-acetyle-γ-butyrolactones and/or 5-substituted 4-acetyl-2(5H)-furanones.
Morpholinium trifluoroacetate-catalyzed aldol condensation of acetone with both aromatic and aliphatic aldehydes
Zumbansen, Kristina,Doehring, Arno,List, Benjamin
experimental part, p. 1135 - 1136 (2010/09/05)
We report a highly efficient, general and practical method for the aldol condensation of acetone with aromatic and aliphatic aldehydes, using morpholinium trifluoroacetate as a catalyst.
Photoreactions in Crystals with Ethenes: Selectivities and Crystal Engineering
Kaupp, Gerd,Frey, Herbert,Behmann, Gabriele
, p. 2135 - 2146 (2007/10/02)
Photoreactions in crystals of sterically hindered dimethylenecyclopentanones 1 and trimethylenecyclopentanes 4 lead to E/Z isomerizations and 1,5-H shifts.The stereochemical result of the photodimerization in the crystalline state of the heterostilbenes 6